rs199542988, FOXRED1

N. diseases: 2
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 1.000 0.040 11 126277489 missense variant G/A;T snv 1.2E-05; 4.0E-06 0.010 1.000 1 2016 2016
Severe psychomotor retardation
CUI: C1854919
Disease: Severe psychomotor retardation
3 1.000 0.040 11 126277489 missense variant G/A;T snv 1.2E-05; 4.0E-06 0.010 1.000 1 2016 2016